Issue 16, 2013

(+)-Fluorenylethylchloroformate (FLEC) – improved synthesis for application in chiral analysis and peptidomimetic synthesis

Abstract

An efficient synthesis of the enantiomers of fluorenylethylchloroformate (FLEC) has been achieved that allows the routine application of the reagent for the resolution of chiral amines including unusual amino acids. The utility of the fluorenylethoxycarbonyl (Feoc) group as a chiral Fmoc equivalent, for combined resolution and protection of amino acids, in solid phase peptide synthesis is also shown.

Graphical abstract: (+)-Fluorenylethylchloroformate (FLEC) – improved synthesis for application in chiral analysis and peptidomimetic synthesis

Supplementary files

Article information

Article type
Communication
Submitted
31 Jan 2013
Accepted
20 Feb 2013
First published
27 Feb 2013

Org. Biomol. Chem., 2013,11, 2571-2573

(+)-Fluorenylethylchloroformate (FLEC) – improved synthesis for application in chiral analysis and peptidomimetic synthesis

M. A. Camerino, D. K. Chalmers and P. E. Thompson, Org. Biomol. Chem., 2013, 11, 2571 DOI: 10.1039/C3OB40218E

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